rs2070615

A SNP in the CACNB3 gene on chromosome 12. Its most notable genotype is A;G: common in complete genomics

Gene
CACNB3
Location
Chr 1248,824,388 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
38%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;GMost notableGoodcommon in complete genomicsTypical · 0.039% of people

On SNPedia: (A;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageA;G 39%
  • European ancestry (Utah)A;G 47%
  • Han Chinese (Beijing)A;G 48%
  • Japanese (Tokyo)A;G 47%
  • Yoruba (Nigeria)A;G 11%
  • African ancestry (Southwest US)A;G 42%
  • Chinese (Denver)A;G 53%
  • Gujarati IndianA;G 48%
  • Luhya (Kenya)A;G 13%
  • Mexican ancestry (Los Angeles)A;G 43%
  • Maasai (Kenya)A;G 31%
  • TuscanA;G 42%

Source and license

Adapted from rs2070615 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.

SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.